Canonical Allele Identifier: CA2155950928

Gene: SERPINA1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94379290_94379291delinsCT , CM000676.2:g.94379290_94379291delinsCT	GRCh38
NC_000014.8:g.94845627_94845628delinsCT , CM000676.1:g.94845627_94845628delinsCT	GRCh37
NC_000014.7:g.93915380_93915381delinsCT	NCBI36
NG_008290.1:g.16402_16403delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393087.9:c.1065+173_1065+174delinsAG MANE Select	ENSP00000376802.4:n.1065+173_1065+174delinsAG
ENST00000636712.1:c.1065+173_1065+174delinsAG	ENSP00000490054.1:n.1065+173_1065+174delinsAG
ENST00000355814.8:c.1065+173_1065+174delinsAG	ENSP00000348068.4:n.1065+173_1065+174delinsAG
ENST00000393087.8:c.1065+173_1065+174delinsAG	ENSP00000376802.4:n.1065+173_1065+174delinsAG
ENST00000393088.8:c.1065+173_1065+174delinsAG	ENSP00000376803.4:n.1065+173_1065+174delinsAG
ENST00000402629.1:c.*158_*159delinsAG	ENSP00000386094.1:n.*158_*159delinsAG
ENST00000404814.8:c.1065+173_1065+174delinsAG	ENSP00000385960.4:n.1065+173_1065+174delinsAG
ENST00000437397.5:c.1065+173_1065+174delinsAG	ENSP00000408474.1:n.1065+173_1065+174delinsAG
ENST00000440909.5:c.1065+173_1065+174delinsAG	ENSP00000390299.1:n.1065+173_1065+174delinsAG
ENST00000448921.5:c.1065+173_1065+174delinsAG	ENSP00000416066.1:n.1065+173_1065+174delinsAG
ENST00000449399.7:c.1065+173_1065+174delinsAG	ENSP00000416354.3:n.1065+173_1065+174delinsAG
ENST00000489769.1:c.*364+173_*364+174delinsAG	ENSP00000451525.1:n.*364+173_*364+174delinsAG
NM_000295.4:c.1065+173_1065+174delinsAG	NP_000286.3:n.1065+173_1065+174delinsAG
NM_001002235.2:c.1065+173_1065+174delinsAG	NP_001002235.1:n.1065+173_1065+174delinsAG
NM_001002236.2:c.1065+173_1065+174delinsAG	NP_001002236.1:n.1065+173_1065+174delinsAG
NM_001127700.1:c.1065+173_1065+174delinsAG	NP_001121172.1:n.1065+173_1065+174delinsAG
NM_001127701.1:c.1065+173_1065+174delinsAG	NP_001121173.1:n.1065+173_1065+174delinsAG
NM_001127702.1:c.1065+173_1065+174delinsAG	NP_001121174.1:n.1065+173_1065+174delinsAG
NM_001127703.1:c.1065+173_1065+174delinsAG	NP_001121175.1:n.1065+173_1065+174delinsAG
NM_001127704.1:c.1065+173_1065+174delinsAG	NP_001121176.1:n.1065+173_1065+174delinsAG
NM_001127705.1:c.1065+173_1065+174delinsAG	NP_001121177.1:n.1065+173_1065+174delinsAG
NM_001127706.1:c.1065+173_1065+174delinsAG	NP_001121178.1:n.1065+173_1065+174delinsAG
NM_001127707.1:c.1065+173_1065+174delinsAG	NP_001121179.1:n.1065+173_1065+174delinsAG
XM_017021370.1:c.1065+173_1065+174delinsAG	XP_016876859.1:n.1065+173_1065+174delinsAG
NM_000295.5:c.1065+173_1065+174delinsAG MANE Select	NP_000286.3:n.1065+173_1065+174delinsAG
NM_001002235.3:c.1065+173_1065+174delinsAG	NP_001002235.1:n.1065+173_1065+174delinsAG
NM_001002236.3:c.1065+173_1065+174delinsAG	NP_001002236.1:n.1065+173_1065+174delinsAG
NM_001127700.2:c.1065+173_1065+174delinsAG	NP_001121172.1:n.1065+173_1065+174delinsAG
NM_001127701.2:c.1065+173_1065+174delinsAG	NP_001121173.1:n.1065+173_1065+174delinsAG
NM_001127702.2:c.1065+173_1065+174delinsAG	NP_001121174.1:n.1065+173_1065+174delinsAG
NM_001127703.2:c.1065+173_1065+174delinsAG	NP_001121175.1:n.1065+173_1065+174delinsAG
NM_001127704.2:c.1065+173_1065+174delinsAG	NP_001121176.1:n.1065+173_1065+174delinsAG
NM_001127705.2:c.1065+173_1065+174delinsAG	NP_001121177.1:n.1065+173_1065+174delinsAG
NM_001127706.2:c.1065+173_1065+174delinsAG	NP_001121178.1:n.1065+173_1065+174delinsAG
NM_001127707.2:c.1065+173_1065+174delinsAG	NP_001121179.1:n.1065+173_1065+174delinsAG